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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1994 Dec;31(12):972–975. doi: 10.1136/jmg.31.12.972

Refinement of the chromosomal position of the X linked juvenile retinoschisis gene.

A A Bergen 1, J B ten Brink 1, L M Bleeker-Wagemakers 1, M J van Schooneveld 1
PMCID: PMC1016703  PMID: 7891384

Abstract

Linkage analysis was carried out in seven X linked juvenile retinoschisis (XLRS) families using four DNA probes and four CA repeat polymorphisms from the Xp22 region. Close linkage was observed between the XLRS locus and DXS207 (theta max = 0.04, Zmax = 3.71), DXS999 (theta max = 0.00, Zmax = 4.59), DXS365 (theta max = 0.07, Zmax = 2.22), and DXS451 (theta max = 0.05, Zmax = 3.26). The analysis of recombination breakpoints and multipoint linkage analysis suggests the order Xpter-DXS16-(DXS43, DXS207)-RS-DXS365-(DXS451, DXS41)-Xcen, thereby refining the position of the XLRS locus to an interval of approximately 3-4 cM. These results improve the feasibility of diagnosis in XLRS considerably, since carriers of this disease cannot be identified clinically.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Alitalo T., Forsius H., Kärnä J., Frants R. R., Eriksson A. W., Wood S., Kruse T. A., de la Chapelle A. Linkage relationships and gene order around the locus for X-linked retinoschisis. Am J Hum Genet. 1988 Oct;43(4):476–483. [PMC free article] [PubMed] [Google Scholar]
  2. Alitalo T., Kruse T. A., de la Chapelle A. Refined localization of the gene causing X-linked juvenile retinoschisis. Genomics. 1991 Mar;9(3):505–510. doi: 10.1016/0888-7543(91)90417-d. [DOI] [PubMed] [Google Scholar]
  3. Arden G. B., Gorin M. B., Polkinghorne P. J., Jay M., Bird A. C. Detection of the carrier state of X-linked retinoschisis. Am J Ophthalmol. 1988 Jun 15;105(6):590–595. doi: 10.1016/0002-9394(88)90049-9. [DOI] [PubMed] [Google Scholar]
  4. Bergen A. A., Samanns C., Schuurman E. J., van Osch L., van Dorp D. B., Pinckers A. J., Bakker E., Gal A., van Ommen G. J., Bleeker-Wagemakers E. M. Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type. Hum Genet. 1991 Dec;88(2):162–166. doi: 10.1007/BF00206065. [DOI] [PubMed] [Google Scholar]
  5. Bergen A. A., Wapenaar M. C., Schuurman E. J., Diergaarde P. J., Lerach H., Monaco A. P., Bakker E., Bleeker-Wagemakers E. M., van Ommen G. J. Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential Alu PCR fingerprint cloning. Cytogenet Cell Genet. 1993;62(4):231–235. doi: 10.1159/000133484. [DOI] [PubMed] [Google Scholar]
  6. Bergen A. A., van Schooneveld M. J., Orth U., Bleeker-Wagemakers E. M., Gal A. Multipoint linkage analysis in X-linked juvenile retinoschisis. Clin Genet. 1993 Mar;43(3):113–116. doi: 10.1111/j.1399-0004.1993.tb04433.x. [DOI] [PubMed] [Google Scholar]
  7. Conneally P. M., Edwards J. H., Kidd K. K., Lalouel J. M., Morton N. E., Ott J., White R. Report of the Committee on Methods of Linkage Analysis and Reporting. Cytogenet Cell Genet. 1985;40(1-4):356–359. doi: 10.1159/000132186. [DOI] [PubMed] [Google Scholar]
  8. Dahl N., Goonewardena P., Chotai J., Anvret M., Pettersson U. DNA linkage analysis of X-linked retinoschisis. Hum Genet. 1988 Mar;78(3):228–232. doi: 10.1007/BF00291666. [DOI] [PubMed] [Google Scholar]
  9. Forsius H., Krause U., Helve J., Vuopala V., Mustonen E., Vainio-Mattila B., Fellman J., Eriksson A. W. Visual acuity in 183 cases of X-chromosomal retinoschisis. Can J Ophthalmol. 1973 Jul;8(3):385–393. [PubMed] [Google Scholar]
  10. Gellert G., Peterson J., Krawczak M., Zoll B. Linkage relationship between retinoschisis and four marker loci. Hum Genet. 1988 Aug;79(4):382–384. doi: 10.1007/BF00282183. [DOI] [PubMed] [Google Scholar]
  11. Sieving P. A., Bingham E. L., Roth M. S., Young M. R., Boehnke M., Kuo C. Y., Ginsburg D. Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes. Am J Hum Genet. 1990 Oct;47(4):616–621. [PMC free article] [PubMed] [Google Scholar]
  12. Weissenbach J., Gyapay G., Dib C., Vignal A., Morissette J., Millasseau P., Vaysseix G., Lathrop M. A second-generation linkage map of the human genome. Nature. 1992 Oct 29;359(6398):794–801. doi: 10.1038/359794a0. [DOI] [PubMed] [Google Scholar]
  13. Wieacker P., Wienker T. F., Dallapiccola B., Bender K., Davies K. E., Ropers H. H. Linkage relationships between Retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosome. Hum Genet. 1983;64(2):143–145. doi: 10.1007/BF00327111. [DOI] [PubMed] [Google Scholar]

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